Please use this identifier to cite or link to this item: http://repo.tma.uz/xmlui/handle/1/5092
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dc.contributor.authorArtikova Dilfuza Maxamatovna-
dc.date.accessioned2026-09-04T15:13:52Z-
dc.date.available2026-09-04T15:13:52Z-
dc.date.issued2026-
dc.identifier.urihttp://repo.tma.uz/xmlui/handle/1/5092-
dc.description.abstractUshbu tadqiqotda COL1A1 rs1800012 T/T genotipi bilan birlamchi “bo‘sh” turk egari sindromining progressiyalanishi o‘rtasidagi bog‘liqlik baholandi. Tadqiqotga birlamchi “bo‘sh” turk egari sindromi bo‘lgan 36 nafar bemor hamda nazorat guruhidagi 36 nafar shaxs jalb etildi. Barcha tekshirilganlarda COL1A1 rs1800012 polimorfizmi bo‘yicha molekulyar genetik tadqiqot o‘tkazildi. Olingan natijalarga ko‘ra, T/T genotipi uchrash chastotasi nazorat guruhidan shakllanayotgan shaklga va undan to‘liq shaklga qarab ortib bordi: 2,8% → 11,8% → 26,3%. Ayniqsa, to‘liq shaklda ushbu genotip bilan sezilarli assotsiatsiya aniqlandi (p=0,01; OR=12,5). Shunday qilib, COL1A1 rs1800012 T/T genotipi birlamchi “bo‘sh” turk egari sindromining to‘liq shakli rivojlanish xavfini baholashda qo‘shimcha molekulyar-genetik marker sifatida qaralishi mumkinen_US
dc.language.isootheren_US
dc.publisherO'zbekiston, Toshkent (ВЕСТНИК) АССОЦИАЦИИ ПУЛЬМОНОЛОГОВ ЦЕНТРАЛЬНОЙ АЗИИ Ежегодный научно-практический журналen_US
dc.relation.ispartofseriesUDC;616.432-007.21:575.113:577.21-
dc.subjectbirlamchi “bo‘sh” turk egari sindromi, BBTE, COL1A1, rs1800012, T/T genotipi, polimorfizm, molekulyar-genetik marker, morfologik progressiyalanish, turk egari diafragmasi.en_US
dc.titleBIRLAMCHI “BO‘SH” TURK EGARI SINDROMINING MORFOLOGIK PROGRESSIYALANISHIDA MOLEKULYAR-GENETIK PREDIKTORLARen_US
dc.typeArticleen_US
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